APA

Dayal B., Salen G., Padia J., Shefer S., Tint G. S., Williams T. H., Toome V. & Sasso G. (19921020). Stereoselective synthesis of (24R and 24S) 5 beta-cholestane-3 alpha,7 alpha,12 alpha,24,25-pentols and (25R and 25S) 5 beta-cholestane-3 alpha,7 alpha,12 alpha,25,26-pentols using a modified osmium-catalyzed Sharpless asymmetric dihydroxylation process. : Chemistry and physics of lipids.

Chicago

Dayal B, Salen G, Padia J, Shefer S, Tint G S, Williams T H, Toome V and Sasso G. 19921020. Stereoselective synthesis of (24R and 24S) 5 beta-cholestane-3 alpha,7 alpha,12 alpha,24,25-pentols and (25R and 25S) 5 beta-cholestane-3 alpha,7 alpha,12 alpha,25,26-pentols using a modified osmium-catalyzed Sharpless asymmetric dihydroxylation process. : Chemistry and physics of lipids.

Harvard

Dayal B., Salen G., Padia J., Shefer S., Tint G. S., Williams T. H., Toome V. and Sasso G. (19921020). Stereoselective synthesis of (24R and 24S) 5 beta-cholestane-3 alpha,7 alpha,12 alpha,24,25-pentols and (25R and 25S) 5 beta-cholestane-3 alpha,7 alpha,12 alpha,25,26-pentols using a modified osmium-catalyzed Sharpless asymmetric dihydroxylation process. : Chemistry and physics of lipids.

MLA

Dayal B, Salen G, Padia J, Shefer S, Tint G S, Williams T H, Toome V and Sasso G. Stereoselective synthesis of (24R and 24S) 5 beta-cholestane-3 alpha,7 alpha,12 alpha,24,25-pentols and (25R and 25S) 5 beta-cholestane-3 alpha,7 alpha,12 alpha,25,26-pentols using a modified osmium-catalyzed Sharpless asymmetric dihydroxylation process. : Chemistry and physics of lipids. 19921020.